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Record Information
Version5.0
StatusDetected but not Quantified
Creation Date2019-10-11 15:33:45 UTC
Update Date2022-03-07 03:18:18 UTC
HMDB IDHMDB0240531
Secondary Accession NumbersNone
Metabolite Identification
Common NameHydroxytyrosol 4'-glucuronide
DescriptionHydroxytyrosol 4'-glucuronide belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose. Based on a literature review very few articles have been published on Hydroxytyrosol 4'-glucuronide.
Structure
Thumb
Synonyms
ValueSource
(2S,3S,4S,5R,6S)-3,4,5-Trihydroxy-6-[2-hydroxy-4-(2-hydroxyethyl)phenoxy]oxane-2-carboxylateHMDB
Chemical FormulaC14H18O9
Average Molecular Weight330.289
Monoisotopic Molecular Weight330.09508216
IUPAC Name(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[2-hydroxy-4-(2-hydroxyethyl)phenoxy]oxane-2-carboxylic acid
Traditional Name(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[2-hydroxy-4-(2-hydroxyethyl)phenoxy]oxane-2-carboxylic acid
CAS Registry NumberNot Available
SMILES
[H][C@@]1(OC2=C(O)C=C(CCO)C=C2)O[C@]([H])(C(O)=O)[C@@]([H])(O)[C@]([H])(O)[C@@]1([H])O
InChI Identifier
InChI=1S/C14H18O9/c15-4-3-6-1-2-8(7(16)5-6)22-14-11(19)9(17)10(18)12(23-14)13(20)21/h1-2,5,9-12,14-19H,3-4H2,(H,20,21)/t9-,10-,11+,12-,14+/m0/s1
InChI KeyJMDNSUMWVYKARS-BYNIDDHOSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.
KingdomOrganic compounds
Super ClassOrganic oxygen compounds
ClassOrganooxygen compounds
Sub ClassCarbohydrates and carbohydrate conjugates
Direct ParentPhenolic glycosides
Alternative Parents
Substituents
  • Phenolic glycoside
  • 1-o-glucuronide
  • O-glucuronide
  • Glucuronic acid or derivatives
  • O-glycosyl compound
  • Tyrosol derivative
  • Phenoxy compound
  • Phenol ether
  • Beta-hydroxy acid
  • Phenol
  • 1-hydroxy-4-unsubstituted benzenoid
  • 1-hydroxy-2-unsubstituted benzenoid
  • Benzenoid
  • Monocyclic benzene moiety
  • Pyran
  • Hydroxy acid
  • Monosaccharide
  • Oxane
  • Secondary alcohol
  • Oxacycle
  • Organoheterocyclic compound
  • Carboxylic acid derivative
  • Carboxylic acid
  • Acetal
  • Polyol
  • Monocarboxylic acid or derivatives
  • Hydrocarbon derivative
  • Primary alcohol
  • Carbonyl group
  • Alcohol
  • Organic oxide
  • Aromatic heteromonocyclic compound
Molecular FrameworkAromatic heteromonocyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
ProcessNot Available
RoleNot Available
Physical Properties
StateNot Available
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
logP-0.79ALOGPS
logP-1.1ChemAxon
logS-1.3ALOGPS
pKa (Strongest Acidic)3.08ChemAxon
pKa (Strongest Basic)-2.4ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count9ChemAxon
Hydrogen Donor Count6ChemAxon
Polar Surface Area156.91 ŲChemAxon
Rotatable Bond Count5ChemAxon
Refractivity73.6 m³·mol⁻¹ChemAxon
Polarizability31.07 ųChemAxon
Number of Rings2ChemAxon
BioavailabilityYesChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DeepCCS[M+H]+166.73830932474
DeepCCS[M-H]-163.44130932474
DeepCCS[M-2H]-198.19730932474
DeepCCS[M+Na]+174.03730932474

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
Hydroxytyrosol 4'-glucuronide[H][C@@]1(OC2=C(O)C=C(CCO)C=C2)O[C@]([H])(C(O)=O)[C@@]([H])(O)[C@]([H])(O)[C@@]1([H])O4477.7Standard polar33892256
Hydroxytyrosol 4'-glucuronide[H][C@@]1(OC2=C(O)C=C(CCO)C=C2)O[C@]([H])(C(O)=O)[C@@]([H])(O)[C@]([H])(O)[C@@]1([H])O3035.9Standard non polar33892256
Hydroxytyrosol 4'-glucuronide[H][C@@]1(OC2=C(O)C=C(CCO)C=C2)O[C@]([H])(C(O)=O)[C@@]([H])(O)[C@]([H])(O)[C@@]1([H])O2939.4Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Hydroxytyrosol 4'-glucuronide,1TMS,isomer #1C[Si](C)(C)OC1=CC(CCO)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]1O2848.2Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,1TMS,isomer #2C[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C12783.5Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,1TMS,isomer #3C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCO)C=C2O)[C@H](O)[C@@H](O)[C@@H]1O2802.9Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,1TMS,isomer #4C[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2=CC=C(CCO)C=C2O)[C@H](O)[C@H]1O2807.2Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,1TMS,isomer #5C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=CC=C(CCO)C=C2O)O[C@H](C(=O)O)[C@H]1O2805.3Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,1TMS,isomer #6C[Si](C)(C)O[C@H]1[C@H](OC2=CC=C(CCO)C=C2O)O[C@H](C(=O)O)[C@@H](O)[C@@H]1O2827.4Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,2TMS,isomer #1C[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C12789.7Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,2TMS,isomer #10C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCO)C=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O2791.0Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,2TMS,isomer #11C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCO)C=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O2788.6Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,2TMS,isomer #12C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCO)C=C2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C2788.9Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,2TMS,isomer #13C[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2=CC=C(CCO)C=C2O)[C@H](O[Si](C)(C)C)[C@H]1O2801.3Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,2TMS,isomer #14C[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2=CC=C(CCO)C=C2O)[C@H](O)[C@H]1O[Si](C)(C)C2795.5Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,2TMS,isomer #15C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](C(=O)O)O[C@@H](OC2=CC=C(CCO)C=C2O)[C@@H]1O[Si](C)(C)C2799.9Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,2TMS,isomer #2C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCO)C=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O2809.1Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,2TMS,isomer #3C[Si](C)(C)OC1=CC(CCO)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O2793.9Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,2TMS,isomer #4C[Si](C)(C)OC1=CC(CCO)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O2795.2Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,2TMS,isomer #5C[Si](C)(C)OC1=CC(CCO)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C2803.5Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,2TMS,isomer #6C[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C12737.1Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,2TMS,isomer #7C[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C12753.4Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,2TMS,isomer #8C[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C12761.1Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,2TMS,isomer #9C[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C12765.5Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TMS,isomer #1C[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C12723.8Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TMS,isomer #10C[Si](C)(C)OC1=CC(CCO)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2793.6Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TMS,isomer #11C[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C12731.2Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TMS,isomer #12C[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C12751.8Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TMS,isomer #13C[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C12733.5Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TMS,isomer #14C[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C12746.6Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TMS,isomer #15C[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C12762.9Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TMS,isomer #16C[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C12754.7Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TMS,isomer #17C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCO)C=C2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O2782.6Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TMS,isomer #18C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCO)C=C2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C2807.1Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TMS,isomer #19C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCO)C=C2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C2787.8Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TMS,isomer #2C[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C12750.8Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TMS,isomer #20C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](OC2=CC=C(CCO)C=C2O)O[C@H](C(=O)O)[C@H]1O[Si](C)(C)C2794.0Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TMS,isomer #3C[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C12767.3Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TMS,isomer #4C[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C12747.2Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TMS,isomer #5C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCO)C=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O2799.4Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TMS,isomer #6C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCO)C=C2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O2784.2Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TMS,isomer #7C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCO)C=C2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C2800.1Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TMS,isomer #8C[Si](C)(C)OC1=CC(CCO)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O2798.3Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TMS,isomer #9C[Si](C)(C)OC1=CC(CCO)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C2805.6Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,4TMS,isomer #1C[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C12773.0Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,4TMS,isomer #10C[Si](C)(C)OC1=CC(CCO)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C2825.7Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,4TMS,isomer #11C[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C12776.2Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,4TMS,isomer #12C[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C12801.6Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,4TMS,isomer #13C[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C12768.0Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,4TMS,isomer #14C[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C12772.5Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,4TMS,isomer #15C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCO)C=C2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C2819.6Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,4TMS,isomer #2C[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C12779.7Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,4TMS,isomer #3C[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C12772.7Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,4TMS,isomer #4C[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C12783.5Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,4TMS,isomer #5C[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C12795.8Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,4TMS,isomer #6C[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C12772.0Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,4TMS,isomer #7C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCO)C=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O2806.9Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,4TMS,isomer #8C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCO)C=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C2830.3Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,4TMS,isomer #9C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCO)C=C2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C2813.2Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,5TMS,isomer #1C[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C12811.4Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,5TMS,isomer #2C[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C12837.8Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,5TMS,isomer #3C[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C12806.0Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,5TMS,isomer #4C[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C12804.8Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,5TMS,isomer #5C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCO)C=C2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C2843.2Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,5TMS,isomer #6C[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C12825.6Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,6TMS,isomer #1C[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C12859.1Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC1=CC(CCO)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]1O3118.4Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C13054.8Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCO)C=C2O)[C@H](O)[C@@H](O)[C@@H]1O3070.1Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2=CC=C(CCO)C=C2O)[C@H](O)[C@H]1O3068.5Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,1TBDMS,isomer #5CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=CC=C(CCO)C=C2O)O[C@H](C(=O)O)[C@H]1O3071.1Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,1TBDMS,isomer #6CC(C)(C)[Si](C)(C)O[C@H]1[C@H](OC2=CC=C(CCO)C=C2O)O[C@H](C(=O)O)[C@@H](O)[C@@H]1O3092.6Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C(C)(C)C)=C13295.6Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,2TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCO)C=C2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O3309.4Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,2TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCO)C=C2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O3288.9Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,2TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCO)C=C2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C3299.7Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,2TBDMS,isomer #13CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2=CC=C(CCO)C=C2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3278.6Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,2TBDMS,isomer #14CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2=CC=C(CCO)C=C2O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3268.1Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,2TBDMS,isomer #15CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](C(=O)O)O[C@@H](OC2=CC=C(CCO)C=C2O)[C@@H]1O[Si](C)(C)C(C)(C)C3275.9Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCO)C=C2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O3307.3Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC1=CC(CCO)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O3294.5Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC1=CC(CCO)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3299.8Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC1=CC(CCO)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3307.5Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C13268.1Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,2TBDMS,isomer #7CC(C)(C)[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)C(O)=C13270.3Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,2TBDMS,isomer #8CC(C)(C)[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(O)=C13276.7Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,2TBDMS,isomer #9CC(C)(C)[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(O)=C13287.0Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C(C)(C)C)=C13495.7Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC1=CC(CCO)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C3499.7Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TBDMS,isomer #11CC(C)(C)[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)C(O)=C13482.6Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TBDMS,isomer #12CC(C)(C)[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(O)=C13481.7Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TBDMS,isomer #13CC(C)(C)[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(O)=C13495.1Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TBDMS,isomer #14CC(C)(C)[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(O)=C13460.9Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TBDMS,isomer #15CC(C)(C)[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(O)=C13482.3Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TBDMS,isomer #16CC(C)(C)[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)C(O)=C13472.5Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TBDMS,isomer #17CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCO)C=C2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O3487.6Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TBDMS,isomer #18CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCO)C=C2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C3520.9Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TBDMS,isomer #19CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCO)C=C2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C3485.0Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)C(O[Si](C)(C)C(C)(C)C)=C13489.6Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TBDMS,isomer #20CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](OC2=CC=C(CCO)C=C2O)O[C@H](C(=O)O)[C@H]1O[Si](C)(C)C(C)(C)C3475.1Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(O[Si](C)(C)C(C)(C)C)=C13502.9Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C13501.0Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCO)C=C2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O3528.9Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCO)C=C2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O3518.2Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCO)C=C2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C3522.5Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC1=CC(CCO)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O3489.2Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC1=CC(CCO)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C3507.8Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)C(O[Si](C)(C)C(C)(C)C)=C13683.5Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,4TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC1=CC(CCO)=CC=C1O[C@@H]1O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C3664.5Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,4TBDMS,isomer #11CC(C)(C)[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(O)=C13647.7Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,4TBDMS,isomer #12CC(C)(C)[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(O)=C13685.5Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,4TBDMS,isomer #13CC(C)(C)[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)C(O)=C13649.5Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,4TBDMS,isomer #14CC(C)(C)[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)C(O)=C13641.6Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,4TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCO)C=C2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C3695.6Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,4TBDMS,isomer #2CC(C)(C)[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(O[Si](C)(C)C(C)(C)C)=C13676.5Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,4TBDMS,isomer #3CC(C)(C)[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C13687.9Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,4TBDMS,isomer #4CC(C)(C)[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(O[Si](C)(C)C(C)(C)C)=C13656.5Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,4TBDMS,isomer #5CC(C)(C)[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C13670.2Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,4TBDMS,isomer #6CC(C)(C)[Si](C)(C)OCCC1=CC=C(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C13658.1Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,4TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCO)C=C2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O3666.2Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,4TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCO)C=C2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C3699.7Semi standard non polar33892256
Hydroxytyrosol 4'-glucuronide,4TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC=C(CCO)C=C2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C3666.3Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Hydroxytyrosol 4'-glucuronide GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Hydroxytyrosol 4'-glucuronide GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Hydroxytyrosol 4'-glucuronide 10V, Positive-QTOFsplash10-000i-0906000000-1e9ddafe0a447e28dcde2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Hydroxytyrosol 4'-glucuronide 20V, Positive-QTOFsplash10-01p9-0922000000-b63ff648d2a6144709132021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Hydroxytyrosol 4'-glucuronide 40V, Positive-QTOFsplash10-0a4i-1900000000-dc9dc93365d73f6d0c132021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Hydroxytyrosol 4'-glucuronide 10V, Negative-QTOFsplash10-004i-0239000000-3e93ff568fc5cd06645b2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Hydroxytyrosol 4'-glucuronide 20V, Negative-QTOFsplash10-000i-3911000000-d265717af7f831f9d2a22021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Hydroxytyrosol 4'-glucuronide 40V, Negative-QTOFsplash10-00di-3910000000-9df95cb99777983b35192021-09-23Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Biological Properties
Cellular LocationsNot Available
Biospecimen Locations
  • Blood
  • Urine
Tissue LocationsNot Available
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
BloodDetected but not QuantifiedNot QuantifiedAdult (>18 years old)BothNormal details
UrineDetected but not QuantifiedNot QuantifiedAdult (>18 years old)BothNormal details
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB093724
KNApSAcK IDNot Available
Chemspider ID62876206
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound102186808
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available